Beckman Coulter recalls UniCel DxH600 hematology analyzers with part number B23858 due to potential sample aspiration problems in open vial positions. Affected units may require correction to prevent inaccurate test results.
The shield for the Single-Tube Station on the DxH instrument may interfere with sample aspiration in the open vial position.
Beckman Coulter is recalling UniCel DxH600 hematology analyzers with part number B23858 because the shield for the Single-Tube Station might interfere with sample aspiration when using open vials. This could lead to inaccurate test results if the instrument is not properly adjusted.
The shield on the Single-Tube Station can interfere with the instrument's ability to properly draw blood samples from open vials. This may cause inaccurate test results if the shield is not correctly positioned or adjusted.
Healthcare facilities using the UniCel DxH600 hematology analyzers with part number B23858 are most at risk. Laboratory staff and patients using the instrument for blood tests may be affected.
Check for the part number B23858 on the UniCel DxH600 hematology analyzer. The instrument is a bench-top unit without a cart or computer stand, and serial number AZ06682 is associated with this recall.
Look for part number B23858 on the UniCel DxH600 hematology analyzer.
No, this recall is for healthcare facilities using the UniCel DxH600 hematology analyzers in clinical settings.
The shield for the Single-Tube Station may interfere with sample aspiration in the open vial position, potentially causing inaccurate test results.
Check for part number B23858 on the UniCel DxH600 hematology analyzer. The instrument is a bench-top unit without a cart or computer stand.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-0237-2018 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-0237-2018 from Beckman Coulter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
